Research ArticleRett Syndrome

mGlu7 potentiation rescues cognitive, social, and respiratory phenotypes in a mouse model of Rett syndrome

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Science Translational Medicine  16 Aug 2017:
Vol. 9, Issue 403, eaai7459
DOI: 10.1126/scitranslmed.aai7459

A positive approach to Rett syndrome

Rett syndrome is an untreatable neurodevelopmental disorder. Gogliotti et al. report a decrease in metabotropic glutamate receptor 7 (mGlu7) expression in brain autopsy samples from patients with Rett syndrome. The authors used in vitro electrophysiological and in vivo pharmacological and behavioral analyses to test whether restoring mGlu7 ameliorated deficits in two Rett syndrome mouse models. mGlu7 reduction disrupted synaptic plasticity in the hippocampus; positive modulation of mGlu7 activity restored synaptic plasticity and reduced cognitive impairments and apneas in the mice. These findings suggest that mGlu7 might be a useful therapeutic target for treating Rett syndrome.


Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the methyl-CpG binding protein 2 (MECP2) gene. The cognitive impairments seen in mouse models of RTT correlate with deficits in long-term potentiation (LTP) at Schaffer collateral (SC)–CA1 synapses in the hippocampus. Metabotropic glutamate receptor 7 (mGlu7) is the predominant mGlu receptor expressed presynaptically at SC-CA1 synapses in adult mice, and its activation on GABAergic interneurons is necessary for induction of LTP. We demonstrate that pathogenic mutations in MECP2 reduce mGlu7 protein expression in brain tissue from RTT patients and in MECP2-deficient mouse models. In rodents, this reduction impairs mGlu7-mediated control of synaptic transmission. We show that positive allosteric modulation of mGlu7 activity restores LTP and improves contextual fear learning, novel object recognition, and social memory. Furthermore, mGlu7 positive allosteric modulation decreases apneas in Mecp2+/− mice, suggesting that mGlu7 may be a potential therapeutic target for multiple aspects of the RTT phenotype.


Rett syndrome (RTT) is an X-linked neurodevelopmental disorder that is caused by loss-of-function mutations in the methyl-CpG binding protein 2 (MECP2) gene (1). Patients with RTT develop relatively normally for the first 6 to 18 months of life, after which they undergo severe developmental regression coinciding with the presentation of seizures, cognitive impairments, apneas, and the loss of language and motor skills (2). Although MECP2 is ubiquitously expressed, almost all symptoms of RTT can be recapitulated when the protein is removed exclusively from the central nervous system in mice (3). Cell-specific knockout and rescue experiments in mice have linked MECP2 deficiency in neuronal subpopulations to distinct aspects of the RTT phenotype, with the most marked effects observed when MECP2 is depleted in GABAergic neurons (48). Among other proposed functions, MECP2 can act to either repress or activate transcription of genes in the brain (9). Hence, several large-scale microarray studies have been performed to identify genes specifically regulated by MECP2 (10, 11). These studies, however, have failed to find gross changes in gene expression and have identified few targets regulated by MECP2 that are amenable to drug development (12, 13).

Metabotropic glutamate receptor 7 (mGlu7) is a heterotrimeric GTP-binding protein–coupled receptor (GPCR) highly expressed in brain regions affected in RTT (14, 15), such as the cortex, hippocampus, striatum, and brainstem (16). mGlu7 is the protein product of the GRM7 gene, which is epigenetically regulated by the methylation status of its promoter (17). mGlu7 is expressed presynaptically at both GABAergic and glutamatergic synapses and acts to decrease neurotransmitter release when stimulated (18, 19). Mouse models of RTT display attenuated long-term potentiation (LTP) at Schaffer collateral (SC)–CA1 synapses in the hippocampus, as well as deficits in hippocampal-based learning and memory tasks consistent with the cognitive impairments present in RTT patients (2022). Because we have previously demonstrated that mGlu7 is necessary for induction of LTP at SC-CA1 (23), we hypothesized that the electrophysiological changes and behavioral deficits observed in RTT model mice could be, in part, due to impaired mGlu7 signaling. This hypothesis is further supported by the fact that mGlu7 knockout mice also display deficits in hippocampal readouts of learning and memory, similarly to RTT animals (24, 25).

Here, we demonstrate that the expression of mGlu7, a GPCR highly amenable to drug development (26), is decreased in the motor cortex of human RTT autopsy samples and in both Mecp2−/y and Mecp2+/− mouse models of RTT. We also show that reduced mGlu7 expression in the hippocampus produces a functional deficit in mGlu7-modulated control of synaptic transmission at SC-CA1 synapses, which can be restored by application of two structurally distinct mGlu7 positive allosteric modulators (PAMs), VU0422288 and VU0155094 (26). Finally, we establish that VU0422288 pretreatment can reverse deficits in contextual fear memory, social recognition, and apneas in RTT model mice. Together, these results suggest that potentiation of mGlu7 may serve as a viable therapeutic approach to treating cognitive and respiratory impairments in RTT.


MECP2 activates GRM7 transcription in vitro

MECP2 was initially identified as a transcriptional repressor; however, it can also activate gene transcription (9). To determine whether MECP2 acts as a transcriptional activator or repressor at the GRM7 locus, we generated a reporter construct containing either 1000 base pairs of the human GRM7 promoter or the minimal pGL4 promoter alone upstream of a luciferase gene (Fig. 1A). Both the minimal promoter and the GRM7-containing constructs were then transfected into human embryonic kidney (HEK) 293 cells with or without human MECP2, and the expression of luciferase was measured by calculating the relative luciferase units (RLU) compared to transfection of a Renilla control vector. We observed no significant change in luciferase expression with the minimal promoter construct with or without MECP2 (Fig. 1B). Conversely, a significant increase in RLU was observed relative to pGL4 alone when the pGL4/GRM7 construct was transfected with either 37.5 or 75.0 ng of MECP2 (P < 0.0001; Fig. 1B), suggesting that MECP2 is an activator at this locus in vitro.

Fig. 1. mGlu7 expression is reduced in RTT autopsy samples.

(A) Diagram of luciferase reporter constructs. (B) Bar graph showing the effect of transfection of increasing amounts of human MECP2 plasmid on luciferase expression from the pGL4 vector with and without the GRM7 promoter [#P < 0.0001 and *P < 0.0001, one-way analysis of variance (ANOVA) with Bonferroni’s post hoc; n = 3]. (C) GRM7 messenger RNA (mRNA) expression in the motor cortex of control and RTT autopsy samples (P = 0.07, two-tailed Student’s t test; n = 7 to 8 biological replicates, df = 13). (D) mGlu7 (***P < 0.0001, two-tailed Student’s t test; n = 7 to 8, df = 13) and (E) vGlut2 (P = 0.39, two-tailed Student’s t test; n = 7 to 8, df = 13) protein expression in control and RTT autopsy samples. (F) Representative Western blots showing mGlu7 and vGlut2 expression in control and RTT motor cortex samples. MECP2 mutations are listed below the representative images.

mGlu7 expression is reduced in human motor cortical tissue

To determine whether our in vitro characterization of MECP2-GRM7 dynamics translated in vivo, we acquired primary motor cortex samples [Brodmann area 4 (BA4)] from seven female patients diagnosed with MECP2 mutation–positive RTT and eight unaffected female control samples matched for age and postmortem interval (table S1). From these samples, we measured GRM7 expression using quantitative real-time polymerase chain reaction (qRT-PCR) and mGlu7 expression using Western blot analysis. We also probed BA4 Western blots for vesicular glutamate transporter 2 (vGlut2) to assess for potential RTT-specific tissue degradation and/or nonspecific increases or decreases in presynaptic proteins. In these experiments, we observed no significant reduction in GRM7 mRNA expression (P = 0.07), a significant decrease in mGlu7 protein (P < 0.001), and no change in vGlut2 expression (Fig. 1, C to F). We previously reported a decrease in MECP2 expression in this sample set (12). These data are in agreement with the hypothesis that MECP2 is an activator of mGlu7 expression and that this relationship is conserved in brain samples from RTT patient autopsy samples.

mGlu7 mRNA and protein expression is reduced in Mecp2−/y mice

We next performed studies to determine whether loss of Mecp2 also results in decreased Grm7 expression in a mouse model of RTT [B6.129P2(C)-Mecp2tm1.1Bird/J; Mecp2−/y], relative to an Mecp2+/y control group, to assess the contribution of decreased mGlu7 to the RTT phenotype (27). In contrast to human motor cortex samples, we detected significantly reduced Grm7 mRNA expression in the total cortex (P < 0.05) and striatum (P < 0.001) of symptomatic Mecp2−/y mice with qRT-PCR {“symptomatic” was defined as the presence of hindlimb clasping and body tremor [postnatal day 39 (P39) to P55]} (Fig. 2A).

Fig. 2. Grm7 and mGlu7 expression is decreased in Mecp2−/y mice.

(A) Grm7 mRNA expression in total cortex (*P < 0.05), hippocampus (P > 0.05), and striatum (***P < 0.001) tissue samples from symptomatic Mecp2−/y mice relative to Mecp2+/y mice (P < 0.0001, two-way ANOVA, genotype × brain region, with Bonferroni’s post hoc; n = 3 to 5, df = 3, 21). (B) Representative Western blots for mGlu7 total protein expression from cortex, hippocampus, and striatum in Mecp2+/y and Mecp2−/y mice. (C) Quantification of mGlu7 total protein expression in the cortex (*P < 0.05), hippocampus (P > 0.05), and striatum (P > 0.05) of Mecp2−/y mice (two-way ANOVA, genotype × brain region, with Bonferroni’s post hoc; n = 7 control and 8 RTT, df = 3, 13). (D) Representative synaptosome Western blots for mGlu7 and vGlut2. (E) Quantification of mGlu7 expression in synaptosomes prepared from cortex (P > 0.05) and hippocampus (***P < 0.001) tissue samples from Mecp2−/y mice. Two-way ANOVA, genotype × brain region with Bonferroni’s post hoc, P < 0.003, n = 5 samples from individual mice, df = 1, 16.

To determine whether mGlu7 protein expression was also decreased, we performed Western blotting on total protein preparations and detected significant reductions in total mGlu7 expression in the cortex (P < 0.05) but not in the hippocampus or striatum (Fig. 2, B and C). The specificity of our mGlu7 antibody was validated using brain tissue from mGlu7 knockout mice (fig. S1). Because functional mGlu7 is expressed presynaptically within the synaptic cleft (16, 18, 19), we also prepared synaptosomes from the cortex and hippocampus to isolate synaptic mGlu7. We observed a significant mGlu7 decrease in hippocampal (P < 0.001), but not cortical, synaptosomes (Fig. 2, D and E), suggesting that the amount of synaptic mGlu7 does not correlate with total cellular mGlu7 in all contexts. To confirm that reductions in Grm7 and mGlu7 were consistent with the loss of Mecp2, we profiled the expression patterns of the known MECP2 target gene glutamate decarboxylase 2 (Gad2; encoding Gad65) (4) as well as of a gene previously shown to be unaffected by Mecp2 mutations, metabotropic glutamate receptor 4 (Grm4; encoding mGlu4). We detected a significant decrease in Gad2 expression but no change in Grm4 expression (fig. S2, A and B) (28). Furthermore, we probed cortical and hippocampal synaptosome blots for vGlut2 and found no change in expression, thereby suggesting that a nonspecific decrease in presynaptic structures is likely not the cause of mGlu7 reduction (Fig. 2D and fig. S2C). Together, these results support the hypothesis that the loss of MECP2 results in a reduction in mGlu7 expression in total cortex and in hippocampal synaptic structures.

Loss of Mecp2 impairs mGlu7 function at SC-CA1 synapses

Application of mGlu7 agonists is known to decrease field excitatory postsynaptic potentials (fEPSPs) at SC-CA1 synapses in rodents (23, 26, 29). To determine whether decreased hippocampal mGlu7 synaptic protein expression correlated with disrupted mGlu7-mediated synaptic transmission, we examined the effects of the agonist LSP4-2022 (30). LSP4-2022 activates mGlu4, mGlu7, and mGlu8; however, we attribute the effects of LSP4-2022 at SC-CA1 synapses to mGlu7 activation because (i) mGlu7 is the only presynaptic mGlu receptor at SC-CA1 synapses in adult mice (26, 31) and (ii) the effects of LSP4-2022 on SC-CA1 synaptic transmission are completely blocked by an mGlu7-selective negative allosteric modulator (NAM), ADX71743 (23, 29). Similar to previous studies (20, 21), we observed altered basal synaptic properties in hippocampal slices from symptomatic Mecp2−/y mice in response to paired-pulse stimulation [0.05 Hz, 20-ms interstimulus interval (ISI)], including an enhanced input-output curve and a reduction in paired-pulse ratio (PPR) (fig. S3). To determine whether there were differences in mGlu7 function in Mecp2−/y mice, we recorded fEPSPs after a 10-min bath application of 30 μM LSP4-2022. In Mecp2+/y slices, LSP4-2022 decreased the slope of the first fEPSP (Fig. 3, A and B). In contrast, LSP4-2022 treatment did not alter the fEPSP slope in Mecp2−/y slices (Fig. 3, A and B). Furthermore, application of LSP4-2022 significantly increased PPR in Mecp2+/y slices (P < 0.01) but had no effect on PPR in Mecp2−/y slices (Fig. 3C).

Fig. 3. mGlu7 function is impaired in Mecp2−/y slices and can be restored by application of VU0422288.

Recordings performed at SC-CA1 synapses. (A) Effect of bath application of LSP4-2022 (blue line) on fEPSP slope in Mecp2+/y and Mecp2−/y slices. Mecp2+/y versus Mecp2−/y [***P < 0.0001, two-tailed Student’s t test; n = 4, 4 (slices, mice), df = 6]. (B) Sample traces of fEPSPs before (1) and during (2) LSP4-2022 treatment in slices from Mecp2+/y and Mecp2−/y mice. (C) PPR after application of LSP4-2022 in Mecp2+/y and Mecp2−/y slices (**P = 0.003, two-tailed paired t test; n = 4, 4, df = 3). n.s., not significant. (D) Effects of pretreatment with VU0422288 alone and in combination with LSP4-2022 in Mecp2−/y slices. Mecp2−/y baseline is from (A). ***P < 0.0001, one-way repeated-measures ANOVA with Bonferonni’s post hoc; n = 4, 4, df = 4, 8. (E) Sample traces of fEPSPs during baseline (1) and after application of VU0422288 and LSP4-2022 (2) in slices from Mecp2−/y mice. (F) PPR after application of VU0422288 and LSP4-2022 in Mecp2−/y slices. P < 0.0001, one-way repeated-measures ANOVA with Bonferonni’s post hoc; n = 5, 5, df = 4, 8. ***P < 0.001 VU0422288 alone versus VU0422288 + LSP4-2022 and ***P < 0.001 VU0422288 + LSP4-2022 versus baseline. (G) Post hoc analysis of PPR comparing baseline Mecp2+/y levels relative to Mecp2−/y baseline (***P < 0.001), VU0422288 alone (***P < 0.001), and VU0422288 + LSP4-2022 (#P < 0.05 relative to Mecp2−/y baseline). Two-tailed Student’s t test. Scale bars, 0.2 mV by 2 ms (B and E).

The loss of LSP4-2022 efficacy in Mecp2−/y brain slices is consistent with an insufficient number of synaptic mGlu7 receptors in the hippocampus to evoke a synaptic depression. To determine whether we could potentiate mGlu7 function, we used two structurally distinct PAMs targeting mGlu7, VU0422288 and VU0155094 (26). This strategy was selected over increasing the concentration of LSP4-2022 to facilitate downstream in vivo experiments, where PAMs can be preferable to agonists for drug development because of their ability to maintain temporal control of receptor activation. VU0422288 and VU0155094 are group III mGlu PAMs that target mGlu4, mGlu7, and mGlu8; however, because of the apparent lack of expression of mGlu4 and mGlu8 at SC-CA1 (31), examining the activity at SC-CA1 should enhance the detection of an mGlu7 component. We have previously shown that both VU0422288 and VU0155094 potentiate the response to 30 μM LSP4-2022 in slices from wild-type C57/B6 mice (26). We pretreated Mecp2−/y slices for 5 min with either 1 μM VU0422288 or 30 μM VU0155094 and then coapplied 1 μM VU0422288 or 30 μM VU0155094 with 30 μM LSP4-2022 for 10 min. Neither VU0422288 nor VU0155094 significantly altered the fEPSP slopes alone, indicating that mGlu7 is not tonically active in Mecp2−/y slices under our stimulation conditions (Fig. 3D and fig. S4, A and B). However, when either PAM was coapplied with LSP4-2022, we observed a significant reduction in the fEPSP slope (P < 0.001; Fig. 3, D and E, and fig. S4, A to C). Additionally, application of either VU0422288 or VU0155094 with LSP4-2022 significantly increased PPR (P < 0.001; Fig. 3, F and G, and fig. S4D). Together, these data indicate that mGlu7 function is reduced in Mecp2−/y slices, consistent with the decrease in receptor expression; however, mGlu7 signaling can be restored with a PAM.

Potentiation of mGlu7 rescues LTP deficits and improves hippocampal learning and memory

Deficits in LTP at SC-CA1 synapses have been observed in several mouse models of RTT (2022). In slices from wild-type C57/B6 mice, we previously found that a high-frequency stimulation (HFS) paradigm induces robust LTP, which can be potentiated by mGlu7 activation (23). In our current experiments, LTP induced by the same HFS was significantly reduced in hippocampal slices from symptomatic Mecp2−/y mice (P < 0.01; fig. S5A). Decreased mGlu7 expression, coupled with our previous report showing that mGlu7 activation is required for LTP at SC-CA1 synapses (23), led us to hypothesize that attenuated LTP in Mecp2−/y slices could be a result of diminished mGlu7 activity. Therefore, we next determined whether potentiation of mGlu7 could rescue LTP. We found that pretreatment of Mecp2−/y slices with 1 μM of the group III mGlu receptor PAM VU0422288 resulted in a complete restoration of the LTP response (fig. S5B). We further examined the effects of VU0422288 using a threshold-HFS protocol in Mecp2+/y slices and found that VU0422288 administration potentiated LTP, suggesting that the observed effects are not genotype-specific (fig. S5, C and D). Together, these data indicate that potentiation of mGlu7 is sufficient to rescue LTP at SC-CA1 synapses in Mecp2−/y mice. Additionally, the finding that application of VU0422288 alone increased fEPSPs after HFS, but not after single pulses (Fig. 3D), indicates that HFS results in sufficient glutamatergic tone at the synapse for a PAM to potentiate mGlu7 function without the need for application of an exogenous agonist.

We next sought to determine whether VU0422288’s effects on LTP translated into improvements in learning and memory. Because the most disease-relevant model of RTT is female Mecp2+/− mice (32), we first assessed whether mGlu7 expression was decreased in these animals. Similar to what was observed in Mecp2−/y mice, we detected a significant decrease in mGlu7 expression in synaptosome preparations from the hippocampus (P < 0.05) but not the cortex (Fig. 4A). We next confirmed an absence of LTP at SC-CA1 in brain slices from 20-week-old Mecp2+/− mice (Fig. 4B), as has previously been reported (33). We found that bath application of VU0422288 could restore LTP at SC-CA1 in this model as well (Fig. 4B). These results provided the rationale to progress to behavioral experiments in Mecp2+/− mice.

Fig. 4. VU0422288 rescues synaptic plasticity defects and learning and memory phenotypes in Mecp2+/− mice.

(A) mGlu7 expression in synaptosome preparations from the cortex (P > 0.05) and hippocampus (*P < 0.05) of Mecp2+/+ and Mecp2+/− mice. n = 7 per genotype, two-tailed Student’s t test. (B) LTP in Mecp2+/+ (filled black circles), Mecp2+/− (*P < 0.05 relative to Mecp2+/+, filled red circles), and Mecp2+/− slices pretreated with VU0422288 (#P < 0.05 relative to Mecp2+/− untreated, empty red circles). The gray bar represents the area from which LTP was measured in the accompanying bar graph. One-way ANOVA with Student’s t test post hoc; n = 4 to 5, 4 (slices, mice). (C) Contextual fear conditioning in Mecp2+/+ and Mecp2+/− mice treated with vehicle (n = 22 and 16), VU0422288 (n = 17 and 15), and ADX88178 (n = 10 and 15). ***P < 0.001, ##P < 0.01, ****P < 0.0001, two-way ANOVA with Student’s t test post hoc analysis; df = 2, 89. # denotes within-genotype comparison. (D) NOR in Mecp2+/+ and Mecp2+/− mice treated with vehicle, VU0422288 and ADX88178. *P < 0.05, #P < 0.05, two-tailed Student’s t test; n = 10 per genotype per treatment. (E) EPM in Mecp2+/+ and Mecp2+/− mice treated with vehicle, VU0422288, and ADX88178. **P < 0.01, *P < 0.05, ##P < 0.01, #P < 0.05, two-tailed Student’s t test; n = 10 per genotype per treatment. * denotes within-treatment comparison, # denotes within-genotype comparison. (F) Social preference assay in Mecp2+/+ and Mecp2+/− mice treated with vehicle, VU0422288, and ADX88178. ***P < 0.001, *P < 0.05, two-tailed Student’s t test, n = 9 to 12 per treatment.

The contextual fear conditioning assay is a behavioral task of learning and memory that relies on proper hippocampal function (34) and has been shown to be attenuated in RTT model mice (21, 35). To assess whether mGlu7 potentiation could improve performance in this task, 18- to 20-week-old female Mecp2+/− mice were given an intraperitoneal injection of vehicle, mGlu4,7,8 PAM VU0422288 (30 mg/kg), or ADX88178 (15 mg/kg) (36) 30 min before training. ADX88178 was chosen as a control for these studies because it is a highly active mGlu4 PAM that also potentiates mGlu8 activity, but not mGlu7 activity, and has been used in both rats and mice for behavioral studies (fig. S6) (36, 37). Using a 10 mg/kg intraperitoneal dose of VU0422288, we measured a total brain concentration of 10.5 μM 1 hour post dose (table S2). The predicted fraction of unbound drug (Fu) for VU0422288 was determined using protein binding assays and was 0.003 in plasma and 0.004 in brain homogenates (that is, 0.3 to 0.4% unbound). The compound exhibited a plasma/brain partitioning coefficient of 1.67 (table S2), resulting in a predicted unbound brain concentration of about 40 nM. Because the in vitro EC50 for VU0422288 is 100 nM (26), we increased the dose to 30 mg/kg to achieve sufficient predicted brain exposure to the compound.

Mice were trained in an operant chamber using two mild foot shocks, and associative learning was quantified as the time spent freezing in the same chamber 24 hours after training. Similar to previous reports, we observed significantly less freezing in vehicle-treated Mecp2+/− mice compared to Mecp2+/+ (P < 0.001; Fig. 4C) (21, 35). Pretreatment with VU0422288 (30 mg/kg) had no effect in Mecp2+/+ animals but resulted in a significant rescue of freezing behavior in Mecp2+/− mice (P < 0.01; Fig. 4C). Pretreatment with ADX88178 (15 mg/kg) had no effect on contextual fear memory in Mecp2+/− mice, suggesting that the observed effects are mGlu7-mediated (Fig. 4C). Nociception in Mecp2+/− mice was comparable to Mecp2+/+ controls, regardless of treatment (fig. S7, A and B).

To assess the effects of mGlu7 potentiation in a cognitive assay not dependent on fear-based memory, we used novel object recognition (NOR). Consistent with previous reports (38), Mecp2+/− mice treated with vehicle 30 min before training failed to distinguish between the novel and familiar objects 1 hour after exposure (Fig. 4D). VU0422288 increased the discrimination index in Mecp2+/− mice to Mecp2+/+ control levels. ADX88178 did not provide the same benefit, again indicating that the effect of VU0422288 are likely mGlu7-mediated (Fig. 4D). Because anxiety can affect both conditioned fear and NOR performance, we also conducted an elevated plus maze (EPM) assay, where increased or decreased time in the open arms is indicative of anxiolytic or anxiogenic phenotypes, respectively. Vehicle-treated Mecp2+/− mice spent significantly more time than Mecp2+/+ control mice in the open arms of the EPM (P < 0.01), and this phenotype was also significantly reversed by VU0422288 (P < 0.05; Fig. 4E). Significant rescue was not observed in ADX88178-treated Mecp2+/− mice relative to vehicle-treated Mecp2+/− mice; however, the significant impairment relative to vehicle-treated Mecp2+/+ mice was lost, likely due to the known effects of mGlu4 and mGlu8 on anxiety (39).

To assess social memory and preference, we performed a three-chamber discrimination assay. In this assay, a mouse is placed in a three-chamber testing box and exposed to a stranger mouse (stranger 1). Three hours later, the mouse is returned to the same chamber and assessed for recognition of stranger 1 relative to a novel mouse (stranger 2). Using the aforementioned compound dosing strategy, Mecp2+/+ control mice demonstrated recognition and preference for the stranger 2 mouse with vehicle, VU0422288, and ADX88178 treatment (Fig. 4F). Conversely, vehicle- and ADX88178-treated Mecp2+/− mice did not distinguish between stranger 1 and stranger 2, indicative of impairments in social recognition and/or preference (Fig. 4F). In contrast, social recognition was normalized in Mecp2+/− mice treated with VU0422288, which demonstrated recognition and preference comparable to Mecp2+/+ controls (Fig. 4F). We further confirmed the role of mGlu7 in both the conditioned fear and social recognition assays by coadministering the group III mGlu PAM VU0422288 with the selective mGlu7 NAM, ADX71743 (29). In these experiments, the benefits of the VU0422288 administration were lost with cotreatment, and mGlu7 NAM–alone treatment disrupted social preference in Mecp2+/+ mice (fig. S8, A to E). These data, coupled with the experiments described above, demonstrate that potentiation of mGlu7 is sufficient to improve impairments in social, cognitive, and anxiety phenotypes in a mouse model of RTT.

The efficacy of VU0422288 is conserved in repeat dosing paradigms

RTT is a lifelong condition, and thus, it is important that pharmacological interventions maintain efficacy along a protracted timeline. To determine whether tolerance would develop with repeat mGlu7 PAM treatment, we administered VU0422288 (30 mg/kg) or vehicle intraperitoneally daily for 17 days in Mecp2+/+ and Mecp2+/− mice. We then conducted EPM, three-chamber social discrimination, and conditioned fear assays at progressive points throughout the dosing paradigm and measured pharmacokinetic properties after the final dose (fig. S9A). Lethality was not observed with any treatment, and both vehicle- and VU0422288-treated Mecp2+/− mice weighed significantly more than Mecp2+/+ controls (P < 0.01 at all time points; fig. S9B). After compound administration on day 17, the pharmacokinetic profile of VU0422288 was comparable between Mecp2+/+ and Mecp2+/− mice, with controls reaching a slightly higher Cmax in the brain (1445 versus 923 ng/g) (fig. S9C). We observed a significant improvement in RTT-like phenotypes in the contextual fear (P < 0.05), EPM (P < 0.05), and three-chamber social preference (P < 0.01) assays in Mecp2+/− mice relative to Mecp2+/+ mice (fig. S9, D to F), suggesting that tolerance did not occur in these studies. Additionally, we detected a loss of social recognition in Mecp2+/+ mice treated subchronically with VU0422288, possibly indicating that mGlu7 potentiation has negative consequences on this phenotype in contexts where mGlu7 expression and/or function is normal.

Potentiation of mGlu7 corrects apneas in Mecp2+/− mice

One primary RTT phenotype that could have translational value as an outcome measure is the presence of both central and obstructive apneas (4042), which occur in 65 to 93% of all RTT patients and are readily quantifiable in Mecp2+/− mice by whole-body plethysmography (WBP). Several studies implicate hyperexcitation of various brainstem nuclei in mediating central apneas (4245), and, in rodents, mGlu7 is expressed in the pons and mesencephalon (46). Given that mGlu7 activation would be predicted to temper glutamatergic tone, we next sought to determine whether mGlu7 potentiation altered this core RTT phenotype. Using the treatment groups described above, we performed WBP to quantify frequency (f), time of inspiration (Ti) and expiration (Te), and apneas over 30 min of motion-free recording in 20- to 22-week-old Mecp2+/− and Mecp2+/+ mice. Irrespective of genotype, both VU0422288 and ADX88178 administration significantly (P < 0.05) decreased breathing rate and increased Ti and Te (Fig. 5, A to C). Because ADX88178 does not potentiate mGlu7, these data suggest that this effect is likely mediated by mGlu4 and/or mGlu8. For all treatment groups, we observed no differences between Mecp2+/+ and Mecp2+/− mice in f, Te, or Ti (Fig. 5, A to C). We observed a marked increase in apneas in vehicle-treated Mecp2+/− mice, which was significantly decreased by a single dose of VU0422288 to a level that was indistinguishable from Mecp2+/+ controls (P < 0.05; Fig. 5, D to F). This benefit was not observed in ADX88178-treated Mecp2+/− mice, again indicating that the effects are mGlu7-mediated (Fig. 5, D to F). Although further work is required to determine the mechanisms responsible for apneas in RTT and where mGlu7 lies in the relevant neurocircuitry, these results provide optimism that mGlu7 modulation may be a viable approach to correct respiratory dysrhythmias and cognitive dysfunction in RTT.

Fig. 5. VU0422288 reduces the number of apneas in Mecp2+/− mice.

WBP. (A) Average breath rate over 30 min in Mecp2+/+ (black) and Mecp2+/− (red) mice in response to vehicle (n = 14 and 11), VU0422288 (n = 11 and 11), and ADX88178 (n = 11 and 14) treatment. ###P < 0.001, #P < 0.05, two-way ANOVA with Student’s t test post hoc. # denotes within-genotype comparison. (B and C) Effects of vehicle, VU0422288, and ADX88178 treatment in Mecp2+/+ and Mecp2+/− mice on (B) inspiration and (C) expiration time. ###P < 0.001, #P < 0.05, two-way ANOVA with Student’s t test post hoc. (D) Quantification of apneas per 10,000 breaths in Mecp2+/+ and Mecp2+/− treated with vehicle, VU0422288, and ADX88178. *P < 0.001, #P < 0.05, two-way ANOVA with Student’s t test post hoc. (E) Sample plethysmography traces.


Since the identification of MECP2 as the causative gene for RTT, there has been considerable effort to identify targets regulated by MECP2 that are amenable to drug development (1). Unfortunately, large-scale microarray studies have identified very few genes regulated by MECP2 that are potential druggable targets (10, 11). Here, we describe reductions in mGlu7 expression in total cortex and at the synaptic level in the hippocampus of Mecp2−/y and Mecp2+/− mice. MECP2 reduction was also observed in autopsy samples from the motor cortex of RTT patients. Decreased synaptic expression of mGlu7 in Mecp2−/y and Mecp2+/− mice translates into a loss of mGlu7 function at SC-CA1 synapses. We found that treatment with two structurally distinct group III mGlu receptor PAMs, VU0422288 and VU0155094, rescued mGlu7-mediated synaptic transmission at SC-CA1 synapses and that VU0422288 administration also rescued learning and memory, social preference, and anxiety phenotypes and reduced apneas in a mouse model of RTT.

Deficits in LTP at SC-CA1 synapses and in behavioral tasks reliant on proper hippocampal function have been well characterized in mouse models of RTT (2022). We previously identified that activation of mGlu7 is a necessary component of LTP induction at SC-CA1 synapses (23). This mechanism is mediated by activation of mGlu7 expressed presynaptically on GABAergic interneurons (23). It has previously been reported that loss of Mecp2 from GABAergic interneurons in mice is sufficient to recapitulate many RTT endophenotypes, including deficits in LTP induction at SC-CA1 (4). Together, these findings suggest that the loss of mGlu7 could be one underlying cause of LTP deficits in mouse models of RTT (2022). We found that potentiation of mGlu7 is able to rescue LTP and improves deficits in hippocampal-dependent contextual fear and social recognition memory assays, indicating that mGlu7 PAMs can be efficacious in vivo.

In addition to the hippocampus, mGlu7 is also expressed in a variety of other brain regions that overlap with the major symptom domains of RTT (16). In rodents, mGlu7 is expressed in brainstem regions implicated in apneas such as the pons and mesencephalon (46), and we show here that potentiation of mGlu7 decreases the presence of apneas in Mecp2+/− mice. Because many intervention strategies that target apneas also have sedative effects (47, 48), the fact that VU0422288 treatment normalizes respiratory phenotypes in the absence of overt sedation in any of our phenotypic assays is a salient finding. When combined with the learning and memory experiments, these studies suggest that modulation of mGlu7 may be a therapeutic strategy for the treatment of several domains of RTT. Furthermore, because the mGlu4,8 PAM (ADX88178) decreased respiratory rate relative to vehicle treatment, these results advocate for the development of selective mGlu7 PAMs, which should be free of this adverse effect.

The dichotomy between GRM7 mRNA and mGlu7 protein expression remains a limitation for these studies that will merit careful consideration in future experiments. Additionally, our experiments in both Mecp2−/y and Mecp2+/− demonstrate that total hippocampal mGlu7 expression is not affected, whereas the functional synaptic pool of mGlu7 is decreased. This may be indicative of a primary deficit in mGlu7 trafficking within RTT model mice; however, our current studies were limited to quantifying expression, and more studies will be required to determine whether this is the case. An additional limitation to our work is that, because of the absence of a selective mGlu7 PAM, we used an mGlu4,7,8 PAM coupled with parallel experiments using an mGlu4,8 PAM and/or an mGlu7 NAM to examine the role of mGlu7 in RTT. Although this strategy suggests that mGlu7 potentiation is beneficial in RTT model mice, it does not exclude the possibility that mGlu4,7 or mGlu7,8 coactivation is required for efficacy. Future work will be required to determine whether mGlu7 potentiation alone is sufficient to explain the results described in this manuscript.

GPCRs such as mGlu7 are considered to be highly druggable targets because their endogenous function is to integrate external signals into intracellular responses upon ligand binding. This is evident by the fact that molecules targeting GPCRs represent 27% of all U.S. Food and Drug Administration–approved drugs (49). Here, we describe how the loss of MECP2 results in decreased mGlu7 signaling and demonstrate that potentiation of mGlu7 function is sufficient to rescue synaptic plasticity deficits and improve multiple RTT-like phenotypes in mice. These data corroborate other studies suggesting that the pathophysiology of RTT is reversible in mouse models (12, 13, 33, 50). Finally, we have shown that mGlu7 expression is sensitive to pathogenic mutations in MECP2, and given that the full range of MECP2-related disorders has only recently been appreciated, it is possible that mGlu7 modulators will have broad utility that extends beyond RTT and into other disorders wherein MECP2 expression and function are compromised, such as MECP2 duplication syndrome and CDKL5 disorder (51, 52).


Study design

On the basis of the localization and known function of mGlu7, we hypothesized that disruptions in mGlu7 signaling were contributing to RTT phenotypes, and our research objectives were to both establish its role at the basic science level and determine whether mGlu7 PAMs could positively modify the disease in rodents. The selection of mouse model, sex, and sample size was based on the standards established by the National Institute of Mental Health and RTT research community (32). For phenotypic assays, mice were assigned randomly to dosing groups, and the quantitation was performed either by a researcher that was blinded to genotype and treatment group or by automated software.

Reporter gene construction and luciferase assay

One thousand base pairs of the GRM7 promoter was cloned into the pGL4 expression vector (Promega), and MECP2 was cloned into the pIRESpuro3 vector (Clontech). MECP2 was transfected into HEK293 cells using FuGENE 6, and luciferase activity was quantified at 48 hours (Promega). The luciferase and Renilla luminescence was measured using a Synergy 2 luminescence plate reader (BioTek). The ratio of luciferase luminescence to Renilla luminescence was calculated and normalized to the control condition with no MECP2 transfection and measured in RLU.


VU0422288, VU0155094, LSP4-2022, ADX88178, and ADX71743 were synthesized at the Vanderbilt Center for Neuroscience Drug Discovery as described in (23, 26, 30). The potency of ADX88178 at mGlu4, mGlu7, and mGlu8 receptors was determined as described in (26).

Quantitative real-time polymerase chain reaction

Total RNA was prepared from Mecp2tm1.1bird (Mecp2−/y) and Mecp2+/y mice and the motor cortex of human samples as described in (12). The Life Technologies gene expression assays used were Grm4 (Mm01306128_m1), Grm7 (Mm0118924_m1), and Gad2 (Mm00484623_m1). Cycle threshold (Ct) values for each sample were normalized to Gapdh (Mm03302249_g1) expression, analyzed using the ΔΔCt method.

Total and synaptosomal protein preparation

For mouse total protein preparation, the cortex, hippocampus, and striatum were microdissected from P39 to P55 Mecp2−/y, 20-week Mecp2+/−, and control mice. For human motor cortex protein preparation, frozen sections were obtained from the University of Maryland Brain and Tissue Bank, which is a Brain and Tissue Repository of the National Institutes of Health NeuroBioBank, and the Harvard Brain Tissue Resource Center, which is supported in part by Public Health Service contract HHSN-271-2013-00030C. Total protein was prepared as described in (12), and synaptosome preparations were prepared as described in (53).

SDS–polyacrylamide gel electrophoresis and fluorescent Western blotting

Mouse (50 μg) and human (96 μg) proteins were electrophoretically separated using a 7% SDS polyacrylamide gel and then transferred onto a nitrocellulose membrane (Bio-Rad). Membranes were blocked in Odyssey blocking buffer (LI-COR) and probed with anti-mGlu7 (1:1000; Upstate), anti-vGlut2 (1:1000; Abcam), or anti-tubulin primary antibody (1:2500; Abcam). The fluorescent secondary antibodies used were goat anti-rabbit (800 nm) (1:5000; LI-COR) and goat anti-mouse (680 nm) (1:5000; LI-COR). Fluorescence was then quantified using the LI-COR Odyssey imaging system. Values were normalized to tubulin and compared relative to controls.

Extracellular field potential recordings

Coronal brain slices were prepared from P45 to P50 Mecp2−/y and 20-week-old Mecp2+/− mice as described in (20). During recordings, slices were continuously perfused with artificial cerebrospinal fluid (Fisher) at 32°C. A concentric bipolar stimulating electrode was positioned near the CA3-CA1 border and paired-pulse fEPSPs were recorded in the stratum radiatum of CA1 (0.05 Hz, 20-ms ISI). For basal synaptic transmission experiments, a stable baseline was recorded for 5 to 10 min before drug application. Dimethyl sulfoxide vehicle, 1 μM VU0422288, or 30 μM VU0155094 was bath-applied for 5 min before the addition of 30 μM LSP4-2022 for 10 min followed by a 15-min washout period.

LTP was induced by applying two trains of 100-Hz stimulation (HFS, 1-s duration, 20-s intertrain interval) after a 15- to 20-min baseline. VU0422288 (1 μM) was applied for 10 min before application of HFS. For all electrophysiological experiments, the slopes of three consecutive sweeps were averaged and normalized to the average slope during the baseline period. Data were digitized using a MultiClamp 700B, Digidata 1322A, and pCLAMP 10 software (Molecular Devices).

In vivo pharmacokinetic analysis

VU0422288 (10 mg/kg) was administered intraperitoneally to adult male Sprague-Dawley rats (Harlan Laboratories). Animals were euthanized at progressive time points and decapitated to obtain blood and brain samples. Liquid chromatography mass spectrometry analysis of plasma and brain VU0422288 concentrations was performed as previously described (26, 30). The brain homogenate binding of VU0422288 was determined in rat brain homogenates via equilibrium dialysis using RED (Rapid Equilibrium Dialysis) plates (Thermo Fisher Scientific).

Compound administration for phenotyping

For all assays, either vehicle (10% Tween 80), VU0422288 (30 mg/kg), ADX88178 (15 mg/kg), a combination of VU0422288 (30 mg/kg) and ADX71743 (60 mg/kg), or ADX71743 (60 mg/kg) was dosed via intraperitoneal injection (10 ml/kg) to 18- to 22-week-old Mecp2+/+ and Mecp2+/− mice (C57/B6, tm1.1 bird allele). Compounds were dosed 30 min before training (contextual fear, novel object, and social preference) or the assay (nociception, EPM, and WBP), such that learning occurred or behavior was assessed at the Tmax of each compound.

Contextual fear conditioning assay

Contextual fear conditioning was performed using a 10% vanilla odor cue and two 1-s, 0.7-mA foot shocks spaced 30 s apart that were preceded by a tone. Associative learning was quantified 24 hours later as the percent time spent freezing in the same chamber containing the odor cue but without the tone or shock. A nociception assay was also performed by applying a series of mild foot shocks of increasing intensity 15 s apart and progressing as follows: 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, and 0.7 mA. Startle response was visually quantified as either a jump or freezing while exploring.

NOR assay

NOR was conducted as described in (54) using the dosing strategy described above. Briefly, mice were placed inside a chamber with two identical objects and allowed to explore for 10 min. The animals were then returned to their home cage. After 1 hour, the mice were placed in the chamber a final time for 10 min, and one of the two objects was replaced with a novel object. The test was video recorded, and the seconds spent directly sniffing each object was scored by a blinded reviewer. Discrimination index was defined as (Timenovel – Timefamiliar)/(Timenovel + Timefamiliar). Direct sniffing in the NOR assay was defined as an approach wherein the mouse’s nose either made contact or came in close proximity to the object. All assays were performed under full light conditions (~400 lux) in 33 cm × 33 cm × 41 cm testing chambers.

Elevated plus maze

For EPM, mice were placed on a T-shaped platform, where two of the arms were closed and two were open. The time spent exploring each arm over a 5-min testing period served as a readout of anxiety behavior. The assay was conducted under full light conditions (~400 lux) in the open arms, and the time spent exploring was quantified by ANY-maze software.

Three-chamber social preference assay

Compound-treated mice were placed in a standard three-chamber apparatus and allowed to habituate for a period of 7 min. The mice were then exposed to a novel juvenile mouse (stranger 1) and a toy rubber duck for 7 min and then returned to their home cage. After 3 hours, the animals were placed back within the three-chamber apparatus, and the time spent in the chamber with stranger 1 or a novel stranger (stranger 2) was quantified for 7 min. Animal tracking was performed using ANY-maze software.

Whole-body plethysmography

Unrestrained Mecp2+/− and Mecp2+/+ mice were placed in a WBP recording chamber (Buxco, two-site system) with a continuous inflow of air (1 liter/min). After a habituation period of 45 min, a baseline recording was established for 30 min. Mice were then removed from the chamber, injected intraperitoneally with compound, and reacclimated for 30 min, and respirator measurements were made for an additional 30 min. Analysis was performed using FinePointe Research Suite (version Apneas, defined as pauses spanning twice the average expiratory time of the previous 2 min, were quantified using the FinePointe apnea software patch, followed by manual spot checking of the larger data set. Only points of motion-free recording were analyzed. Periods of movement were removed (i) automatically by the FinePointe apnea software, (ii) manually by identifying points where the Δ-chamber volume exceeded the normal breath range, and (iii) at points where the researcher present during the recording noted activity. All filters were applied while the researchers were blinded to genotype and treatment group.

Statistical analyses

Statistics were carried out using Prism 6.0 (GraphPad) and Excel (Microsoft). Data for all graphs are presented in their respective figure legends. All data shown represent means ± SEM. Statistical significance between groups was determined using two-tailed unpaired or paired Student’s t tests and one- or two-way ANOVA, with Bonferroni’s or individual Student’s t test post hoc analysis. Sample size, number of replicates, and statistical test are specified in each figure legend.


Materials and Methods

Fig. S1. Antibody #07-239 is selective for mGlu7.

Fig. S2. Gad65, but not mGlu4, expression is reduced in Mecp2−/y mice.

Fig. S3. Mecp2−/y hippocampal slices display enhanced excitatory transmission at the SC-CA1 synapse.

Fig. S4. VU0155094, a PAM that is structurally distinct from VU0422288, also rescues the efficacy of LSP4-2022 on fEPSPs at SC-CA1 in Mecp2−/y slices.

Fig. S5. VU0422288 rescues attenuated LTP at the SC-CA1 synapse in Mecp2−/y mice.

Fig. S6. ADX88178 is active at mGlu4 and mGlu8, but not at mGlu7.

Fig. S7. Startle response threshold is not affected by VU0422288 and ADX88178 treatment in Mecp2+/+ or Mecp2+/− mice.

Fig. S8. Coadministration of VU0422288 and ADX71743 confirm mGlu7’s role in cognition but evokes sedative effects.

Fig. S9. Efficacy is conserved with repeated VU0422288 administration.

Table S1. Human motor cortex sample data.

Table S2. Pharmacokinetic analysis of VU0422288.


Acknowledgments: We acknowledge the donation of samples from RTT patient families, and we thank the University of Maryland Brain and Tissue Bank, the Harvard Brain Tissue Resource Center, and, for their assistance in obtaining this valuable resource. Funding: R.G.G. was supported by a postdoctoral fellowship from, NIH T32 AG000260, and NIH T32-MH065215. R.K.S. was supported by a Weatherstone Predoctoral Fellowship from Autism Speaks and the Howard Hughes Medical Institute Certificate Program in Molecular Medicine through Vanderbilt University. N.M.F. was supported by training grant NIH T32 GM007628-36 and the Vanderbilt Program in Molecular Medicine through Vanderbilt University. A.G.W. was supported by a postdoctoral fellowship through the PhRMA Foundation. We also acknowledge U54 MH084659 (C.W.L.), R01 NS031373 (P.J.C.), a Basic Research grant from (C.M.N.), a Treatment Grant from Autism Speaks (C.M.N.), and R21 MH102548 (C.M.N.). Author contributions: R.G.G., R.K.S., N.M.F., A.G.W., and C.M.N. designed, performed, and analyzed the molecular, phenotypic, and electrophysiology experiments. R.Z. and C.M.N. performed and analyzed the in vitro pharmacology assays, and J.A. and R.G.G. performed the WBP assays. A.L.B. and J.S.D. conducted the LC MS/MS, plasma binding, and protein binding experiments for DMPK analysis, and D.W.E. and C.R.H. synthesized the compounds used herein. C.K.J. assisted in the design of behavioral assays, C.W.L. oversaw chemical optimization, Z.X., P.J.C., and C.M.N. supervised electrophysiology experiments, and P.J.C. and C.M.N. oversaw molecular pharmacology experiments. R.G.G., R.K.S., and C.M.N. wrote and edited the paper with input from all authors. Competing interests: The authors declare that they have no competing interests. Data and materials availability: The data for each graph have been presented in the figure legends and in the body of the text.
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